Cholesterol Medication Is Being Recalled Nationwide—Over 140,000 Bottles Affected

Oct 24, 2025 | Uncategorized

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Danielle DeAngelis

Getty Images. EatingWell design.

Key Points

  • At least 141,984 bottles of cholesterol medication are being recalled nationwide.

  • The prescription impacted is Atorvastatin Calcium tablets sold in 90-count, 500-count and 1000-count packages.

  • Contact your healthcare provider or pharmacy for a potential refund or replacement.

The U.S. Food and Drug Administration announced a recall on prescription statin medication sold nationwide. This is due to “failed dissolution specifications.”

The drugs impacted by this recall are Atorvastatin Calcium tablets manufactured by Ascend Laboratories, LLC. At least 141,984 bottles of the product are affected. Below is the list of cholesterol medication being recalled, including lot codes and expiration dates that can be found on the bottles or packaging:

Product Description

Pill Count

Lot Numbers

Expiration Dates

Atorvastatin Calcium Tablets USP, 10 mg

90-count; 500-count 1000-count

25141249; 24144938; 24144868; 24144867; 24144458; 24143994; 24142987; 24143316

Feb. 2027; Nov. 2026; Sept. 2026; July 2026

Atorvastatin Calcium Tablets USP, 40 mg, Rx Only

90-count; 500-count 1000-count

25140933; 25140477; 24144254; 24144163; 24143995

Feb. 2027; Dec. 2026; Oct. 2026; Sept. 2026

Atorvastatin Calcium Tablets USP, 20 mg, Rx Only

90-count; 500-count 1000-count

25140150; 25140173; 25140172; 24144720; 24144798; 24144692; 24143755; 24143913; 24143754; 24143047; 24142936

Dec. 2026, Nov. 2026; Oct. 2026; Aug. 2026; July 2026; June 2026

Atorvastatin Calcium Tablets USP, 80 mg, Rx Only

90-count, 500-count

25140249; 25140247; 24144999; 24144942; 24144845; 24144713; 24144652; 24143898; 24143412; 24143582

Dec. 2026; Nov. 2026; Oct. 2026; Aug. 2026

Check your medication, and if it matches any of the above recall information, contact your healthcare provider or pharmacy for a replacement or potential refund. This recall was just classified as a Class II, meaning that the recalled tablets may lead to minor, temporary health problems.

For questions about this recall, contact the FDA at 1-888-INFO-FDA (1-888-463-6332).

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